Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 727935생성일: 2026년 10월 26일
Triethylamine → 6-Fluoro-1-(4-fluorophenyl)-1,4-dihydro-4-oxo-7-(5-benzyl-2,5-diazabicyclo(2.2.1)hept-2-yl)quinoline-3-carboxylic acid
https://huagongshe.com/reaction/727935
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2-Benzyl-2,5-diazabicyclo[2.2.1]heptane | HCID 562932 | — |
| 반응물 | 6,7-Difluoro-1-(4-fluorophenyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 10448622 | — |
| 반응물 | HCID 178506430 | HCID 178506430 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 6-Fluoro-1-(4-fluorophenyl)-1,4-dihydro-4-oxo-7-(5-benzyl-2,5-diazabicyclo(2.2.1)hept-2-yl)quinoline-3-carboxylic acid | HCID 14014823 | 63% |
반응 단계
To a solution of 1.5 g (4 m Mol) of the mixed anhydride of 6,7-difluoro-1-(4-fluorophenyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid with difluoroboronic acid in 10 ml of dimethylsulfoxide was added 0.9 g (4.78 m Mol) 2-benzyl-2.5-diazabicyclo(2.2.1)heptane and 0.4 g (4 m Mol) of triethylamine. After stirring for 4 hrs at room temperature, 150 ml of ether was added and the crystals that formed were collected by filtration. The residue was heated in a mixture of 60 ml dioxane and 90 ml 1.5N NaOH and heated at 100° C. for 1 hr. The hot solution was filtered to removed non-dissolved material. The solution was neutralized with conc HCl and the resultant crystals collected, washed with water and left to dry in the air. After recrystallization from DMF, 1.23 g (63%) of the product was obtained, mp 275° -280° dec.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05045549 |
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| 출처 데이터셋 | uspto-grants-1991_09 |
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| ORD ID | ord-7473c576eeb74db383a97732f181e25b |
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| 출처 메모 | uspto-grants-1991_09 |
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